Restrictive cardiomyopathy due to storage disease (Q96351): Difference between revisions
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15 August 2026
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Latest revision as of 12:19, 16 August 2026
Restrictive cardiomyopathy due to storage disease is the presence of restrictive cardiomyopathy in the presence of a glycogen, sphingolipidoses (such as α-galactosidase-A deficiency (Anderson-Fabry disease)), mucopolysaccharidoses (such as α-l iduronidase deficiency (Hurler syndrome)), iron-overload (such as haemochromatosis), or other storage disorder known to be significantly associated with restrictive cardiomyopathy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1721344709 |
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| English | Restrictive cardiomyopathy due to storage disease |
Restrictive cardiomyopathy due to storage disease is the presence of restrictive cardiomyopathy in the presence of a glycogen, sphingolipidoses (such as α-galactosidase-A deficiency (Anderson-Fabry disease)), mucopolysaccharidoses (such as α-l iduronidase deficiency (Hurler syndrome)), iron-overload (such as haemochromatosis), or other storage disorder known to be significantly associated with restrictive cardiomyopathy. |
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CID11:ID_1721344709
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dki-india-ID_1721344709
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Concluído
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15 August 2026
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